Human (GRCh37.p13)
Description

family with sequence similarity 219, member A [Source:HGNC Symbol;Acc:19920]

Gene Synonyms

C9orf25, FLJ39031, bA573M23.5

Location

Chromosome 9: 34,398,182-34,458,568 reverse strand.

GRCh37:CM000671.1

About this gene

This gene has 9 transcripts (splice variants) and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000445726.1FAM219A-2013644185aaENSP00000392452.1
 
Protein coding
CCDS55304Q5T593 Q8IW50 NM_001184941.1GENCODE basic
ENST00000379089.1FAM219A-0013624183aaENSP00000368382.1
 
Protein coding
--GENCODE basic
ENST00000379080.1FAM219A-0073591172aaENSP00000368371.1
 
Protein coding
-NM_001184942.1GENCODE basic
ENST00000297620.4FAM219A-0083588168aaENSP00000297620.4
 
Protein coding
CCDS6556Q8IW50 NM_147202.1GENCODE basic
ENST00000379087.1FAM219A-0023573166aaENSP00000368380.1
 
Protein coding
--GENCODE basic
ENST00000379081.1FAM219A-0043543156aaENSP00000368372.1
 
Protein coding
-NM_001184945.1GENCODE basic
ENST00000379084.1FAM219A-003893164aaENSP00000368377.1
 
Protein coding
Q5T586 -GENCODE basic
ENST00000422409.1FAM219A-005798168aaENSP00000409737.1
 
Protein coding
Q5T593 -CDS 3' incomplete
ENST00000379078.1FAM219A-006770156aaENSP00000368369.1
 
Protein coding
--GENCODE basic